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hal.structure.identifierEnvironnements et Paléoenvironnements OCéaniques [EPOC]
dc.contributor.authorTOMAZ, Sophie
hal.structure.identifierMax Planck Institute for Chemistry [MPIC]
dc.contributor.authorSHAHPOURY, Pourya
hal.structure.identifierLaboratoire de glaciologie et géophysique de l'environnement [LGGE]
dc.contributor.authorJAFFREZO, Jean-Luc
hal.structure.identifierMasaryk University [Brno] [MUNI]
hal.structure.identifierMax Planck Institute for Chemistry [MPIC]
dc.contributor.authorLAMMEL, Gerhard
hal.structure.identifierEnvironnements et Paléoenvironnements OCéaniques [EPOC]
dc.contributor.authorPERRAUDIN, Emilie
hal.structure.identifierEnvironnements et Paléoenvironnements OCéaniques [EPOC]
dc.contributor.authorVILLENAVE, Eric
hal.structure.identifierInstitut National de l'Environnement Industriel et des Risques [INERIS]
dc.contributor.authorALBINET, Alexandre
dc.date.accessioned2024-05-14T13:07:43Z
dc.date.available2024-05-14T13:07:43Z
dc.date.issued2016-05
dc.identifier.issn0048-9697
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/199827
dc.description.abstractEn21 PAHs, 27 oxy-PAHs and 32 nitro-PAHs were measured every third day over a year in both gaseous (G) and particulate PM10 (P) phases in ambient air of Grenoble (France). Mean total concentrations (G + P) of PAHs and oxy-PAHs were in the same range and about 10 ng m− 3. Nitro-PAHs were 50 to 100 times less concentrated averaging 100 pg m− 3. Polycyclic aromatic compound (PAC) concentrations were 5 to 7 times higher in “cold” period (October to March) than in “warm” period (April to September). Seasonal variations may be explained by higher primary emissions from residential heating, especially biomass burning in “cold” season. Meteorological conditions and influence of the geomorphology around Grenoble, with the formation of thermal inversion layers leading to the stagnation of pollutants, were additional key parameters. Maximum individual PAC concentrations were observed during two PM10 pollution events in December and February–March. Chemical processes and secondary formation of oxy- and nitro-PAH were probably enhanced by the accumulation of the pollutants during these events. PAC gas/particle partitioning depended on compound molecular weight and vapour pressure. Gas/particle partitioning of oxy- and nitro-PAHs were evaluated using a multi-phase poly-parameter linear free energy relationship model. The PAC cancer risk was assessed using toxic equivalency factors available in the literature (19 PAHs, 10 nitro-PAHs and 1 oxy-PAH). Overall, particle-bound PACs contributed about 76% of the cancer risk. While PAHs accounted for most of the total PAC cancer risk, oxy- and nitro-PAHs could account for up to 24%. The risk quantification across substance classes is limited by toxicological data availability.
dc.language.isoen
dc.publisherElsevier
dc.subject.enPAH
dc.subject.enOPAH
dc.subject.enNPAH
dc.subject.enGas/particle partitioning model
dc.subject.enAerosol
dc.subject.enAir quality
dc.title.enOne-year study of polycyclic aromatic compounds at an urban site in Grenoble (France): Seasonal variations, gas/particle partitioning and cancer risk estimation
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.scitotenv.2016.05.137
dc.subject.halSciences de l'environnement
bordeaux.journalScience of the Total Environmenten_US
bordeaux.page1071–1083
bordeaux.volume565
bordeaux.hal.laboratoriesEPOC : Environnements et Paléoenvironnements Océaniques et Continentaux - UMR 5805en_US
bordeaux.institutionUniversité de Bordeaux
bordeaux.institutionCNRS
bordeaux.peerReviewedoui
bordeaux.import.sourcehal
hal.identifierinsu-01387781
hal.version1
hal.popularnon
hal.audienceInternationale
hal.exportfalse
workflow.import.sourcehal
dc.rights.ccPas de Licence CCen_US
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